S26R (p.Ser26Arg) variant of FGFR2 (P21802)
S26R (p.Ser26Arg) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
S26R (p.Ser26Arg) variant details
- p.Ser26Arg
- gnomAD rs1466576334
- Missense
- Variant Prioritization Score for Impact Estimate 0.259
- REVEL 0.16
- CADD 23.00
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available